Unknown

Dataset Information

0

Ancestral L-amino acid oxidases for deracemization and stereoinversion of amino acids.


ABSTRACT: L-amino acid oxidases (LAAOs) can be applied to convert racemic amino acids to D-isomers, which are potential precursors of pharmaceuticals. However, this application is hampered by the lack of available stable and structure-determined LAAOs. In this study, we attempt to address this limitation by utilizing two ancestral LAAOs: AncLAAO-N4 and AncLAAO-N5. AncLAAO-N4 has the highest thermal and temporal stabilities among the designed LAAOs that can be used for deracemization and stereoinversion. AncLAAO-N5 can provide X-ray crystal structures, which are helpful to reveal substrate recognition and reaction mechanisms of LAAOs at the molecular level. Next, we attempted to improve activity of AncLAAO-N4 toward L-Val through a semi-rational protein engineering method. Three variants with enhanced activity toward L-Val were obtained. Taken together, we believe that the activity and substrate selectivity of AncLAAOs give them the potential to be key enzymes in various chemoenzymatic reactions.

SUBMITTER: Nakano S 

PROVIDER: S-EPMC9814856 | biostudies-literature | 2020 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

Ancestral L-amino acid oxidases for deracemization and stereoinversion of amino acids.

Nakano Shogo S   Kozuka Kohei K   Minamino Yuki Y   Karasuda Hiroka H   Hasebe Fumihito F   Ito Sohei S  

Communications chemistry 20201204 1


L-amino acid oxidases (LAAOs) can be applied to convert racemic amino acids to D-isomers, which are potential precursors of pharmaceuticals. However, this application is hampered by the lack of available stable and structure-determined LAAOs. In this study, we attempt to address this limitation by utilizing two ancestral LAAOs: AncLAAO-N4 and AncLAAO-N5. AncLAAO-N4 has the highest thermal and temporal stabilities among the designed LAAOs that can be used for deracemization and stereoinversion. A  ...[more]

Similar Datasets

| S-EPMC4499246 | biostudies-literature
| S-EPMC9072125 | biostudies-literature
| S-EPMC522121 | biostudies-literature
| S-EPMC7797136 | biostudies-literature
| S-EPMC3971498 | biostudies-literature
| S-EPMC9844085 | biostudies-literature
| S-EPMC8159540 | biostudies-literature
| S-EPMC7052187 | biostudies-literature
2019-03-11 | GSE114855 | GEO
| S-EPMC11396064 | biostudies-literature